부분 구조 검색

421798

Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57284
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(F)c(CN2CCNc3ncc(-c4cnc(N5CCNCC5)nc4)nc32)c1Cl
Reaction #167722
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1268141
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2cc(-c3cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc3)c(F)cc2s1
Reaction #1622998
DOI: 10.1039/C8SC04228D
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1654426
DOI: 10.1039/C8SC04228D
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1815020
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #1908493
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2cc(-c3cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc3)c(F)cc2s1
Reaction #2155870
desired product
수율 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(N3CCc4ccc(-c5cnc(N6CCN(C(=O)OC(C)(C)C)CC6)nc5)cc4C3)nc(N)n2)CC1
Reaction #2177468
tert-Butyl 4-(5-{2-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-1,2,3,4-tetrahydroisoquinolin-7-yl}-pyrimidin-2-yl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(N3CCc4ccc(-c5cnc(N6CCN(C(=O)OC(C)(C)C)CC6)nc5)cc4C3)nc(N)n2)CC1
Reaction #2221717
DOI: 10.1039/C8SC04228D
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #2431265
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nn3c(-c4cnc(N5CCN(C(=O)OC(C)(C)C)CC5)nc4)cnc3s2)cc1OC
Reaction #2496737
desired product
수율 102.5%DOI: 10.6084/m9.figshare.5104873.v1